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: A0A3S7X1Y8
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 | 130 | 134 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.491 |
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.332 |
CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 589 | 593 | PF00656 | 0.582 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.501 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.691 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.691 |
CLV_PCSK_PC7_1 | 226 | 232 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 57 | 61 | PF00082 | 0.377 |
DEG_APCC_DBOX_1 | 372 | 380 | PF00400 | 0.464 |
DEG_APCC_DBOX_1 | 523 | 531 | PF00400 | 0.594 |
DEG_SCF_FBW7_2 | 48 | 53 | PF00400 | 0.398 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.595 |
DOC_CKS1_1 | 413 | 418 | PF01111 | 0.495 |
DOC_MAPK_gen_1 | 108 | 115 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 353 | 359 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 391 | 397 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 419 | 426 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 341 | 348 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 419 | 426 | PF00069 | 0.537 |
DOC_PP1_RVXF_1 | 39 | 46 | PF00149 | 0.460 |
DOC_PP4_FxxP_1 | 413 | 416 | PF00568 | 0.418 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 525 | 528 | PF00568 | 0.630 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.277 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.415 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 182 | 189 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 617 | 624 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 100 | 116 | PF00022 | 0.500 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.623 |
LIG_BRCT_BRCA1_1 | 74 | 78 | PF00533 | 0.562 |
LIG_Clathr_ClatBox_1 | 201 | 205 | PF01394 | 0.496 |
LIG_EVH1_2 | 596 | 600 | PF00568 | 0.542 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.407 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.475 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.606 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.531 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.482 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.364 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.638 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.437 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.315 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.364 |
LIG_FHA_2 | 118 | 124 | PF00498 | 0.532 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.426 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.473 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.363 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.620 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.351 |
LIG_LIR_Apic_2 | 410 | 416 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 211 | 222 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 82 | 92 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 479 | 484 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.281 |
LIG_MAD2 | 651 | 659 | PF02301 | 0.363 |
LIG_MYND_1 | 528 | 532 | PF01753 | 0.624 |
LIG_Pex14_1 | 374 | 378 | PF04695 | 0.379 |
LIG_Pex14_2 | 56 | 60 | PF04695 | 0.466 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.409 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.403 |
LIG_SH2_CRK | 481 | 485 | PF00017 | 0.496 |
LIG_SH2_CRK | 67 | 71 | PF00017 | 0.368 |
LIG_SH2_GRB2like | 334 | 337 | PF00017 | 0.455 |
LIG_SH2_PTP2 | 85 | 88 | PF00017 | 0.474 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.346 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.530 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 20 | 26 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 198 | 205 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 570 | 577 | PF11976 | 0.612 |
LIG_TRAF2_1 | 267 | 270 | PF00917 | 0.366 |
LIG_TRFH_1 | 85 | 89 | PF08558 | 0.357 |
LIG_TYR_ITAM | 211 | 228 | PF00017 | 0.440 |
LIG_WRC_WIRS_1 | 206 | 211 | PF05994 | 0.474 |
LIG_WRC_WIRS_1 | 587 | 592 | PF05994 | 0.517 |
MOD_CDK_SPxxK_3 | 412 | 419 | PF00069 | 0.497 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.557 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.554 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.322 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.550 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.227 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.732 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.734 |
MOD_CK1_1 | 386 | 392 | PF00069 | 0.425 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.343 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.571 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.522 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.650 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.510 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.496 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.667 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.451 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.647 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.315 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.609 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.549 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.747 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.700 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.803 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.602 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.723 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.677 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.724 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.767 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.430 |
MOD_GlcNHglycan | 434 | 438 | PF01048 | 0.643 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.509 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.468 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.606 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.586 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.438 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.342 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.716 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.730 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.643 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.672 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.581 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.393 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.434 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.568 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.487 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.350 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.520 |
MOD_N-GLC_1 | 665 | 670 | PF02516 | 0.562 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.632 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.372 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.442 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.731 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.378 |
MOD_PIKK_1 | 491 | 497 | PF00454 | 0.599 |
MOD_PK_1 | 144 | 150 | PF00069 | 0.593 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.481 |
MOD_PKA_2 | 616 | 622 | PF00069 | 0.358 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.595 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.615 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.386 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.516 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.522 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.510 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.610 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.322 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.367 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.454 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.337 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.762 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.490 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.482 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.376 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.322 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.356 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.416 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.736 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.527 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.571 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.500 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.450 |
MOD_SUMO_for_1 | 178 | 181 | PF00179 | 0.658 |
MOD_SUMO_rev_2 | 337 | 342 | PF00179 | 0.371 |
TRG_DiLeu_BaEn_4 | 269 | 275 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.414 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.450 |
TRG_DiLeu_BaLyEn_6 | 498 | 503 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.631 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.400 |
TRG_NLS_MonoExtN_4 | 226 | 233 | PF00514 | 0.615 |
TRG_Pf-PMV_PEXEL_1 | 482 | 487 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCH8 | Leptomonas seymouri | 66% | 100% |
A0A0S4IV50 | Bodo saltans | 34% | 100% |
A0A1X0NS55 | Trypanosomatidae | 38% | 100% |
A0A3R7REE6 | Trypanosoma rangeli | 34% | 100% |
A4HGU7 | Leishmania braziliensis | 83% | 100% |
A4I3X5 | Leishmania infantum | 100% | 100% |
D0A943 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B065 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q820 | Leishmania major | 95% | 100% |
V5BC43 | Trypanosoma cruzi | 36% | 100% |