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: A4HGU7
Term | Name | Level | Count |
---|---|---|---|
GO:0008152 | metabolic process | 1 | 8 |
GO:0009058 | biosynthetic process | 2 | 7 |
GO:0002183 | cytoplasmic translational initiation | 4 | 1 |
GO:0006413 | translational initiation | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 8 |
GO:0016779 | nucleotidyltransferase activity | 4 | 8 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003743 | translation initiation factor activity | 4 | 1 |
GO:0005085 | guanyl-nucleotide exchange factor activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0008135 | translation factor activity, RNA binding | 3 | 1 |
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 | 272 | 276 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 365 | 369 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 592 | 596 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 356 | 358 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.500 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 356 | 358 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.667 |
CLV_PCSK_PC7_1 | 226 | 232 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.325 |
DEG_APCC_DBOX_1 | 375 | 383 | PF00400 | 0.458 |
DEG_SCF_FBW7_2 | 48 | 53 | PF00400 | 0.331 |
DOC_CKS1_1 | 416 | 421 | PF01111 | 0.504 |
DOC_MAPK_FxFP_2 | 528 | 531 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 108 | 115 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 356 | 362 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 394 | 400 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 344 | 351 | PF00069 | 0.470 |
DOC_PP1_RVXF_1 | 39 | 46 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.584 |
DOC_PP4_FxxP_1 | 416 | 419 | PF00568 | 0.427 |
DOC_PP4_FxxP_1 | 528 | 531 | PF00568 | 0.617 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.616 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.405 |
LIG_14-3-3_CanoR_1 | 182 | 189 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 348 | 352 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 527 | 531 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 620 | 627 | PF00244 | 0.443 |
LIG_Actin_WH2_2 | 100 | 116 | PF00022 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BRCT_BRCA1_1 | 74 | 78 | PF00533 | 0.487 |
LIG_Clathr_ClatBox_1 | 201 | 205 | PF01394 | 0.483 |
LIG_EVH1_2 | 599 | 603 | PF00568 | 0.525 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.380 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.482 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.626 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.343 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.768 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.417 |
LIG_FHA_1 | 620 | 626 | PF00498 | 0.311 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.395 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.331 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.507 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.631 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.266 |
LIG_LIR_Apic_2 | 413 | 419 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 211 | 222 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.261 |
LIG_LIR_Gen_1 | 82 | 92 | PF02991 | 0.238 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 482 | 487 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 529 | 533 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.221 |
LIG_MAD2 | 654 | 662 | PF02301 | 0.368 |
LIG_MYND_1 | 531 | 535 | PF01753 | 0.612 |
LIG_Pex14_1 | 377 | 381 | PF04695 | 0.370 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.411 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.385 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.381 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.488 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.281 |
LIG_SH2_GRB2like | 337 | 340 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 271 | 275 | PF00017 | 0.463 |
LIG_SH2_PTP2 | 85 | 88 | PF00017 | 0.411 |
LIG_SH2_SRC | 271 | 274 | PF00017 | 0.318 |
LIG_SH2_SRC | 337 | 340 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.281 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.426 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.525 |
LIG_SH3_3 | 594 | 600 | PF00018 | 0.548 |
LIG_SUMO_SIM_anti_2 | 20 | 26 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 132 | 139 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 573 | 580 | PF11976 | 0.622 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.368 |
LIG_TRFH_1 | 85 | 89 | PF08558 | 0.281 |
LIG_TYR_ITAM | 211 | 228 | PF00017 | 0.408 |
LIG_WRC_WIRS_1 | 206 | 211 | PF05994 | 0.458 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.295 |
LIG_WRC_WIRS_1 | 590 | 595 | PF05994 | 0.455 |
MOD_CDK_SPxxK_3 | 415 | 422 | PF00069 | 0.505 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.305 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.544 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.346 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.706 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.339 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.580 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.612 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.522 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.411 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.753 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.494 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.307 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.622 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.546 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.746 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.673 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.587 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.678 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.720 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.626 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.421 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.653 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.484 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.614 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.427 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.499 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.679 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.730 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.459 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.653 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.733 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.629 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.442 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.544 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.431 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.384 |
MOD_N-GLC_1 | 409 | 414 | PF02516 | 0.499 |
MOD_N-GLC_1 | 668 | 673 | PF02516 | 0.563 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.442 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.574 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.547 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.480 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.376 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.416 |
MOD_NEK2_2 | 389 | 394 | PF00069 | 0.339 |
MOD_NEK2_2 | 55 | 60 | PF00069 | 0.184 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.469 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.714 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.385 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.595 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.504 |
MOD_PKA_2 | 347 | 353 | PF00069 | 0.478 |
MOD_PKA_2 | 526 | 532 | PF00069 | 0.723 |
MOD_PKA_2 | 619 | 625 | PF00069 | 0.351 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.448 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.558 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.620 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.449 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.507 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.496 |
MOD_Plk_4 | 131 | 137 | PF00069 | 0.518 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.305 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.350 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.336 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.770 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.479 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.425 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.370 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.431 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.412 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.591 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.732 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.509 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 236 | 242 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_4 | 272 | 278 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 396 | 401 | PF01217 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 501 | 506 | PF01217 | 0.700 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 484 | 487 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.281 |
TRG_ER_diArg_1 | 242 | 245 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 356 | 358 | PF00400 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 485 | 489 | PF00026 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCH8 | Leptomonas seymouri | 66% | 100% |
A0A0S4IV50 | Bodo saltans | 32% | 100% |
A0A1X0NS55 | Trypanosomatidae | 37% | 100% |
A0A3R7REE6 | Trypanosoma rangeli | 34% | 100% |
A0A3S7X1Y8 | Leishmania donovani | 83% | 100% |
A4I3X5 | Leishmania infantum | 83% | 100% |
D0A943 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B065 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q820 | Leishmania major | 83% | 100% |
V5BC43 | Trypanosoma cruzi | 34% | 100% |