Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 2 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0018444 | translation release factor complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8ICH2
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003924 | GTPase activity | 7 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005525 | GTP binding | 5 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0019001 | guanyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003747 | translation release factor activity | 5 | 1 |
GO:0008079 | translation termination factor activity | 4 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 681 | 683 | PF00675 | 0.308 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.228 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 395 | 397 | PF00082 | 0.225 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.227 |
DEG_SPOP_SBC_1 | 261 | 265 | PF00917 | 0.642 |
DOC_ANK_TNKS_1 | 731 | 738 | PF00023 | 0.508 |
DOC_CKS1_1 | 146 | 151 | PF01111 | 0.571 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.712 |
DOC_CYCLIN_yCln2_LP_2 | 707 | 713 | PF00134 | 0.508 |
DOC_MAPK_gen_1 | 191 | 200 | PF00069 | 0.581 |
DOC_MAPK_gen_1 | 202 | 208 | PF00069 | 0.599 |
DOC_MAPK_gen_1 | 312 | 323 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 496 | 505 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 526 | 533 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 732 | 740 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 496 | 503 | PF00149 | 0.427 |
DOC_PP1_RVXF_1 | 634 | 641 | PF00149 | 0.383 |
DOC_PP2B_LxvP_1 | 401 | 404 | PF13499 | 0.427 |
DOC_PP2B_LxvP_1 | 537 | 540 | PF13499 | 0.424 |
DOC_PP4_FxxP_1 | 549 | 552 | PF00568 | 0.407 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.697 |
DOC_USP7_MATH_2 | 213 | 219 | PF00917 | 0.638 |
DOC_USP7_UBL2_3 | 282 | 286 | PF12436 | 0.640 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.583 |
DOC_USP7_UBL2_3 | 558 | 562 | PF12436 | 0.499 |
DOC_USP7_UBL2_3 | 675 | 679 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 717 | 721 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 396 | 401 | PF00244 | 0.469 |
LIG_APCC_ABBA_1 | 713 | 718 | PF00400 | 0.470 |
LIG_APCC_ABBAyCdc20_2 | 80 | 86 | PF00400 | 0.645 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.574 |
LIG_BIR_III_2 | 233 | 237 | PF00653 | 0.622 |
LIG_BIR_III_4 | 402 | 406 | PF00653 | 0.427 |
LIG_BRCT_BRCA1_1 | 597 | 601 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_2 | 597 | 603 | PF00533 | 0.458 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.613 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.427 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.427 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.427 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.693 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.794 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.757 |
LIG_FHA_2 | 278 | 284 | PF00498 | 0.619 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.508 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.427 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.427 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.481 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.469 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.385 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.420 |
LIG_FHA_2 | 597 | 603 | PF00498 | 0.323 |
LIG_FXI_DFP_1 | 716 | 720 | PF00024 | 0.245 |
LIG_IRF3_LxIS_1 | 422 | 428 | PF10401 | 0.427 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.595 |
LIG_LIR_Apic_2 | 546 | 552 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 366 | 373 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 474 | 483 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 670 | 680 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 718 | 727 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 670 | 676 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 718 | 722 | PF02991 | 0.508 |
LIG_PCNA_APIM_2 | 722 | 728 | PF02747 | 0.427 |
LIG_Pex14_1 | 365 | 369 | PF04695 | 0.427 |
LIG_Pex14_2 | 319 | 323 | PF04695 | 0.445 |
LIG_Pex14_2 | 434 | 438 | PF04695 | 0.427 |
LIG_REV1ctd_RIR_1 | 638 | 648 | PF16727 | 0.508 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.677 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.427 |
LIG_SH2_GRB2like | 24 | 27 | PF00017 | 0.616 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.618 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.427 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.699 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 122 | 125 | PF00017 | 0.712 |
LIG_SH2_STAT3 | 139 | 142 | PF00017 | 0.418 |
LIG_SH2_STAT3 | 28 | 31 | PF00017 | 0.625 |
LIG_SH2_STAT3 | 49 | 52 | PF00017 | 0.532 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.334 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.560 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.582 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.728 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.481 |
LIG_SUMO_SIM_par_1 | 423 | 429 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 644 | 649 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 708 | 714 | PF11976 | 0.508 |
LIG_SxIP_EBH_1 | 624 | 636 | PF03271 | 0.368 |
LIG_TRAF2_1 | 212 | 215 | PF00917 | 0.686 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.638 |
LIG_TRAF2_1 | 288 | 291 | PF00917 | 0.509 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.470 |
LIG_TRAF2_1 | 666 | 669 | PF00917 | 0.427 |
LIG_UBA3_1 | 459 | 465 | PF00899 | 0.445 |
LIG_UBA3_1 | 530 | 538 | PF00899 | 0.508 |
LIG_UBA3_1 | 676 | 683 | PF00899 | 0.508 |
MOD_CDK_SPxxK_3 | 285 | 292 | PF00069 | 0.635 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.661 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.741 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.427 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.445 |
MOD_CK1_1 | 595 | 601 | PF00069 | 0.447 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.345 |
MOD_CK1_1 | 655 | 661 | PF00069 | 0.508 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.690 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.621 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.662 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.530 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.427 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.435 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.448 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.348 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.372 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.357 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.508 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.427 |
MOD_Cter_Amidation | 200 | 203 | PF01082 | 0.605 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.716 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.682 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.640 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.706 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.571 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.227 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.328 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.517 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.308 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.308 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.643 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.776 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.669 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.445 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.369 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.340 |
MOD_GSK3_1 | 742 | 749 | PF00069 | 0.433 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.520 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.621 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.427 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.441 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.415 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.644 |
MOD_PIKK_1 | 256 | 262 | PF00454 | 0.749 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.427 |
MOD_PKA_1 | 396 | 402 | PF00069 | 0.427 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.427 |
MOD_PKA_2 | 396 | 402 | PF00069 | 0.427 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.508 |
MOD_PKB_1 | 302 | 310 | PF00069 | 0.621 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.445 |
MOD_Plk_2-3 | 541 | 547 | PF00069 | 0.421 |
MOD_Plk_2-3 | 592 | 598 | PF00069 | 0.364 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.520 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.438 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.421 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.445 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.656 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.668 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.740 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.778 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.765 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 228 | 231 | PF00179 | 0.653 |
MOD_SUMO_for_1 | 296 | 299 | PF00179 | 0.524 |
MOD_SUMO_rev_2 | 221 | 230 | PF00179 | 0.720 |
MOD_SUMO_rev_2 | 467 | 472 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 532 | 540 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 559 | 563 | PF00179 | 0.493 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 566 | 569 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 396 | 398 | PF00400 | 0.426 |
TRG_NLS_Bipartite_1 | 191 | 206 | PF00514 | 0.684 |
TRG_NLS_MonoExtN_4 | 190 | 195 | PF00514 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 615 | 619 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAZ5 | Leptomonas seymouri | 80% | 100% |
A0A1X0NV54 | Trypanosomatidae | 71% | 100% |
A0A3R7MLL0 | Trypanosoma rangeli | 70% | 100% |
A0A3S7X9T0 | Leishmania donovani | 30% | 100% |
A4H6P3 | Leishmania braziliensis | 89% | 100% |
A4HN87 | Leishmania braziliensis | 31% | 100% |
A4HV24 | Leishmania infantum | 99% | 100% |
A4IBV5 | Leishmania infantum | 30% | 100% |
C9ZYQ4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A7C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AFP2 | Leishmania major | 32% | 100% |
E9AGP5 | Leishmania infantum | 36% | 100% |
E9ANQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B6U5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O13354 | Candida albicans | 41% | 100% |
O74718 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 39% | 100% |
P23637 | Ogataea pini | 40% | 100% |
Q4QGW5 | Leishmania major | 94% | 100% |
Q5R6Y0 | Pongo abelii | 37% | 100% |
Q69ZS7 | Mus musculus | 35% | 100% |
Q6AXM7 | Rattus norvegicus | 36% | 100% |
Q9HGI6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 39% | 100% |
Q9HGI7 | Candida maltosa | 38% | 100% |
Q9W074 | Drosophila melanogaster | 35% | 100% |
Q9Y450 | Homo sapiens | 37% | 100% |