Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 9 |
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: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 20 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 21 |
GO:0016020 | membrane | 2 | 21 |
GO:0110165 | cellular anatomical entity | 1 | 21 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A0A3S7WV81
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0016197 | endosomal transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 21 |
GO:0005488 | binding | 1 | 21 |
GO:0005525 | GTP binding | 5 | 21 |
GO:0017076 | purine nucleotide binding | 4 | 21 |
GO:0019001 | guanyl nucleotide binding | 5 | 21 |
GO:0032553 | ribonucleotide binding | 3 | 21 |
GO:0032555 | purine ribonucleotide binding | 4 | 21 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 21 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 21 |
GO:0036094 | small molecule binding | 2 | 21 |
GO:0043167 | ion binding | 2 | 21 |
GO:0043168 | anion binding | 3 | 21 |
GO:0097159 | organic cyclic compound binding | 2 | 21 |
GO:0097367 | carbohydrate derivative binding | 2 | 21 |
GO:1901265 | nucleoside phosphate binding | 3 | 21 |
GO:1901363 | heterocyclic compound binding | 2 | 21 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 197 | 201 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.424 |
CLV_Separin_Metazoa | 234 | 238 | PF03568 | 0.462 |
CLV_Separin_Metazoa | 254 | 258 | PF03568 | 0.296 |
DEG_APCC_DBOX_1 | 185 | 193 | PF00400 | 0.393 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.430 |
DEG_SCF_FBW7_1 | 586 | 593 | PF00400 | 0.830 |
DEG_SPOP_SBC_1 | 506 | 510 | PF00917 | 0.710 |
DEG_SPOP_SBC_1 | 525 | 529 | PF00917 | 0.561 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.392 |
DOC_CKS1_1 | 587 | 592 | PF01111 | 0.751 |
DOC_CYCLIN_RxL_1 | 123 | 135 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 70 | 76 | PF00134 | 0.380 |
DOC_MAPK_gen_1 | 172 | 179 | PF00069 | 0.427 |
DOC_MAPK_gen_1 | 306 | 313 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 186 | 194 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 322 | 329 | PF00069 | 0.413 |
DOC_PP4_FxxP_1 | 144 | 147 | PF00568 | 0.445 |
DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.380 |
DOC_SPAK_OSR1_1 | 372 | 376 | PF12202 | 0.485 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.852 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.829 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.834 |
DOC_USP7_UBL2_3 | 333 | 337 | PF12436 | 0.417 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.816 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.814 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.835 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.840 |
DOC_WW_Pin1_4 | 586 | 591 | PF00397 | 0.688 |
LIG_14-3-3_CanoR_1 | 153 | 157 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 555 | 561 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 65 | 71 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 209 | 227 | PF00022 | 0.417 |
LIG_Actin_WH2_2 | 390 | 408 | PF00022 | 0.469 |
LIG_APCC_ABBA_1 | 190 | 195 | PF00400 | 0.380 |
LIG_APCC_ABBA_1 | 426 | 431 | PF00400 | 0.639 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.706 |
LIG_BIR_III_4 | 200 | 204 | PF00653 | 0.441 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.450 |
LIG_BRCT_BRCA1_1 | 493 | 497 | PF00533 | 0.663 |
LIG_EH_1 | 414 | 418 | PF12763 | 0.761 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.392 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.472 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.522 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.659 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.683 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.674 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.493 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.384 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.799 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.662 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.378 |
LIG_FXI_DFP_1 | 357 | 361 | PF00024 | 0.378 |
LIG_LIR_Apic_2 | 262 | 267 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 175 | 184 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 188 | 199 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 272 | 278 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 48 | 57 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 64 | 73 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 99 | 107 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 175 | 179 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 211 | 216 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 359 | 363 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 79 | 84 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.382 |
LIG_NRBOX | 284 | 290 | PF00104 | 0.547 |
LIG_PCNA_yPIPBox_3 | 421 | 429 | PF02747 | 0.657 |
LIG_Pex14_1 | 264 | 268 | PF04695 | 0.467 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.385 |
LIG_Pex14_2 | 209 | 213 | PF04695 | 0.434 |
LIG_Pex14_2 | 273 | 277 | PF04695 | 0.455 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.382 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.411 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.359 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.393 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 176 | 179 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.437 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.424 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 546 | 549 | PF00017 | 0.567 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.403 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.499 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.454 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.745 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.635 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.676 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.790 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.759 |
LIG_SUMO_SIM_anti_2 | 152 | 159 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 279 | 287 | PF11976 | 0.538 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.604 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.578 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.508 |
LIG_TRAF2_1 | 589 | 592 | PF00917 | 0.700 |
LIG_TRAF2_2 | 293 | 298 | PF00917 | 0.465 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 366 | 371 | PF05994 | 0.355 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.342 |
LIG_WW_3 | 254 | 258 | PF00397 | 0.474 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.273 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.606 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.709 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.754 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.699 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.635 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.582 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.357 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.827 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.843 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.406 |
MOD_CK2_1 | 586 | 592 | PF00069 | 0.834 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.378 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.623 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.680 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.672 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.723 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.755 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.784 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.821 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.822 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.833 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.393 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.412 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.500 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.625 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.732 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.687 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.627 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.838 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.839 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.819 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.724 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.741 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.387 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.393 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.472 |
MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.497 |
MOD_N-GLC_2 | 178 | 180 | PF02516 | 0.322 |
MOD_N-GLC_2 | 612 | 614 | PF02516 | 0.635 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.440 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.364 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.493 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.519 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.549 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.723 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.743 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.860 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.655 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.428 |
MOD_NEK2_2 | 424 | 429 | PF00069 | 0.571 |
MOD_NEK2_2 | 66 | 71 | PF00069 | 0.393 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.472 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.380 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.656 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.815 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.437 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.628 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.402 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.633 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.378 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.464 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.826 |
MOD_Plk_2-3 | 152 | 158 | PF00069 | 0.486 |
MOD_Plk_2-3 | 45 | 51 | PF00069 | 0.495 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.412 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.394 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.491 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.458 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.402 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.436 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.617 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.687 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.408 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.836 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.394 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.385 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.416 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.819 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.859 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.703 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.840 |
MOD_ProDKin_1 | 586 | 592 | PF00069 | 0.687 |
MOD_SUMO_rev_2 | 274 | 282 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 418 | 423 | PF00179 | 0.652 |
TRG_DiLeu_BaEn_1 | 152 | 157 | PF01217 | 0.505 |
TRG_DiLeu_BaEn_1 | 185 | 190 | PF01217 | 0.402 |
TRG_DiLeu_BaEn_1 | 280 | 285 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.549 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.215 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.547 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.532 |
TRG_NES_CRM1_1 | 280 | 295 | PF08389 | 0.532 |
TRG_NLS_MonoExtC_3 | 334 | 340 | PF00514 | 0.413 |
TRG_NLS_MonoExtN_4 | 333 | 339 | PF00514 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 206 | 210 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8K7 | Leptomonas seymouri | 78% | 100% |
A0A0N0P9A4 | Leptomonas seymouri | 44% | 100% |
A0A0S4KGM0 | Bodo saltans | 63% | 100% |
A0A1X0P6D7 | Trypanosomatidae | 63% | 100% |
A0A1X0P9Q8 | Trypanosomatidae | 45% | 100% |
A0A3R7LDF3 | Trypanosoma rangeli | 60% | 100% |
A0A3S7X801 | Leishmania donovani | 46% | 100% |
A0A422P0G8 | Trypanosoma rangeli | 45% | 100% |
A4H9Y5 | Leishmania braziliensis | 75% | 100% |
A4HAT9 | Leishmania braziliensis | 46% | 100% |
A4HY50 | Leishmania infantum | 100% | 100% |
A4IA07 | Leishmania infantum | 46% | 100% |
D0A0F1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9ARX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9B513 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4Q2X3 | Leishmania major | 46% | 100% |
Q4QDJ3 | Leishmania major | 92% | 100% |
Q4V8H8 | Rattus norvegicus | 34% | 100% |
Q8BH64 | Mus musculus | 34% | 100% |
Q9NZN4 | Homo sapiens | 34% | 100% |
V5BSA9 | Trypanosoma cruzi | 60% | 100% |
V5DGT0 | Trypanosoma cruzi | 44% | 100% |