Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
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. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005851 | eukaryotic translation initiation factor 2B complex | 2 | 1 |
GO:0032045 | guanyl-nucleotide exchange factor complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9B065
Term | Name | Level | Count |
---|---|---|---|
GO:0002183 | cytoplasmic translational initiation | 4 | 1 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003743 | translation initiation factor activity | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005085 | guanyl-nucleotide exchange factor activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016779 | nucleotidyltransferase activity | 4 | 7 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0030695 | GTPase regulator activity | 4 | 1 |
GO:0045182 | translation regulator activity | 1 | 1 |
GO:0060589 | nucleoside-triphosphatase regulator activity | 3 | 1 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:0140677 | molecular function activator activity | 2 | 1 |
GO:0140678 | molecular function inhibitor activity | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:0008879 | glucose-1-phosphate thymidylyltransferase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.320 |
CLV_C14_Caspase3-7 | 449 | 453 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 588 | 592 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.678 |
CLV_PCSK_PC7_1 | 226 | 232 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.365 |
DEG_APCC_DBOX_1 | 371 | 379 | PF00400 | 0.449 |
DEG_APCC_DBOX_1 | 522 | 530 | PF00400 | 0.585 |
DEG_SCF_FBW7_2 | 48 | 53 | PF00400 | 0.376 |
DEG_SPOP_SBC_1 | 284 | 288 | PF00917 | 0.570 |
DOC_CKS1_1 | 412 | 417 | PF01111 | 0.474 |
DOC_MAPK_gen_1 | 108 | 115 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 352 | 358 | PF00069 | 0.395 |
DOC_MAPK_gen_1 | 390 | 396 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 418 | 425 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 418 | 425 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 39 | 46 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.559 |
DOC_PP4_FxxP_1 | 412 | 415 | PF00568 | 0.397 |
DOC_PP4_FxxP_1 | 524 | 527 | PF00568 | 0.618 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 632 | 636 | PF00917 | 0.342 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.417 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.432 |
LIG_14-3-3_CanoR_1 | 182 | 189 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 399 | 407 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 616 | 623 | PF00244 | 0.430 |
LIG_Actin_WH2_2 | 100 | 116 | PF00022 | 0.508 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 74 | 78 | PF00533 | 0.562 |
LIG_Clathr_ClatBox_1 | 201 | 205 | PF01394 | 0.484 |
LIG_EVH1_2 | 595 | 599 | PF00568 | 0.520 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.384 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.490 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.584 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.511 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.381 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.465 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.385 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.721 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.409 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.298 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.392 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.565 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.406 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.477 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.316 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.616 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.348 |
LIG_LIR_Apic_2 | 409 | 415 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 211 | 222 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 82 | 92 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 478 | 483 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.273 |
LIG_MAD2 | 650 | 658 | PF02301 | 0.351 |
LIG_MYND_1 | 527 | 531 | PF01753 | 0.608 |
LIG_Pex14_1 | 373 | 377 | PF04695 | 0.363 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.455 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.382 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.386 |
LIG_SH2_CRK | 480 | 484 | PF00017 | 0.470 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.357 |
LIG_SH2_GRB2like | 333 | 336 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 85 | 88 | PF00017 | 0.470 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.340 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.524 |
LIG_SH3_3 | 590 | 596 | PF00018 | 0.542 |
LIG_SUMO_SIM_anti_2 | 20 | 26 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 569 | 576 | PF11976 | 0.608 |
LIG_TRAF2_1 | 266 | 269 | PF00917 | 0.337 |
LIG_TRFH_1 | 85 | 89 | PF08558 | 0.349 |
LIG_TYR_ITAM | 211 | 228 | PF00017 | 0.409 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.251 |
LIG_WRC_WIRS_1 | 206 | 211 | PF05994 | 0.455 |
LIG_WRC_WIRS_1 | 586 | 591 | PF05994 | 0.447 |
MOD_CDK_SPxxK_3 | 411 | 418 | PF00069 | 0.477 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.546 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.310 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.529 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.349 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.571 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.708 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.382 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.304 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.536 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.554 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.633 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.519 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.489 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.757 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.465 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.594 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.298 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.605 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.533 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.696 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.806 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.592 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.710 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.677 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.718 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.612 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.593 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.415 |
MOD_GlcNHglycan | 433 | 437 | PF01048 | 0.616 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.479 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.790 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.584 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.438 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.735 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.726 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.417 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.661 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.731 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.621 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.371 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.415 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.541 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.421 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.377 |
MOD_N-GLC_1 | 664 | 669 | PF02516 | 0.548 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.682 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.358 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.408 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.708 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.359 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.602 |
MOD_PK_1 | 144 | 150 | PF00069 | 0.585 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.478 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.339 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.588 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.430 |
MOD_Plk_1 | 385 | 391 | PF00069 | 0.506 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.554 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.493 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.601 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.310 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.347 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.446 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.327 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.766 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.481 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.416 |
MOD_Plk_4 | 617 | 623 | PF00069 | 0.356 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.424 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.454 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.399 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.739 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.735 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.480 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.440 |
TRG_DiLeu_BaEn_1 | 269 | 274 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.432 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 480 | 483 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.340 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 352 | 354 | PF00400 | 0.383 |
TRG_NLS_MonoExtN_4 | 226 | 233 | PF00514 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 481 | 486 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCH8 | Leptomonas seymouri | 66% | 100% |
A0A0S4IV50 | Bodo saltans | 31% | 100% |
A0A1X0NS55 | Trypanosomatidae | 38% | 100% |
A0A3R7REE6 | Trypanosoma rangeli | 35% | 100% |
A0A3S7X1Y8 | Leishmania donovani | 93% | 100% |
A4HGU7 | Leishmania braziliensis | 82% | 100% |
A4I3X5 | Leishmania infantum | 93% | 100% |
D0A943 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
Q4Q820 | Leishmania major | 95% | 100% |
V5BC43 | Trypanosoma cruzi | 36% | 100% |