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:0005840 | ribosome | 5 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 9 |
Related structures:
AlphaFold database: A4HEZ5
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0008270 | zinc ion binding | 6 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.621 |
CLV_C14_Caspase3-7 | 36 | 40 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.294 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.633 |
CLV_Separin_Metazoa | 329 | 333 | PF03568 | 0.593 |
DEG_APCC_DBOX_1 | 326 | 334 | PF00400 | 0.336 |
DEG_APCC_DBOX_1 | 400 | 408 | PF00400 | 0.385 |
DOC_ANK_TNKS_1 | 360 | 367 | PF00023 | 0.484 |
DOC_CYCLIN_RxL_1 | 514 | 526 | PF00134 | 0.395 |
DOC_MAPK_gen_1 | 156 | 164 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 64 | 71 | PF00069 | 0.620 |
DOC_MAPK_HePTP_8 | 61 | 73 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 64 | 73 | PF00069 | 0.566 |
DOC_MAPK_RevD_3 | 143 | 158 | PF00069 | 0.515 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 425 | 429 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.546 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 148 | 154 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 427 | 433 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 520 | 530 | PF00244 | 0.411 |
LIG_Actin_WH2_2 | 64 | 79 | PF00022 | 0.445 |
LIG_AP2alpha_2 | 218 | 220 | PF02296 | 0.448 |
LIG_APCC_ABBA_1 | 217 | 222 | PF00400 | 0.546 |
LIG_BRCT_BRCA1_1 | 420 | 424 | PF00533 | 0.434 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.270 |
LIG_deltaCOP1_diTrp_1 | 469 | 479 | PF00928 | 0.546 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.473 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.522 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.656 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.640 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.483 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.569 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.403 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.418 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.513 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.696 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.568 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.470 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.407 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.534 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 198 | 202 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 326 | 331 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 528 | 537 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 469 | 475 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.549 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.593 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.488 |
LIG_SH2_STAT3 | 181 | 184 | PF00017 | 0.570 |
LIG_SH2_STAT3 | 515 | 518 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.472 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.530 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.536 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.606 |
LIG_SUMO_SIM_anti_2 | 496 | 502 | PF11976 | 0.301 |
LIG_SUMO_SIM_par_1 | 159 | 166 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 302 | 307 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 499 | 505 | PF11976 | 0.297 |
LIG_SxIP_EBH_1 | 268 | 277 | PF03271 | 0.449 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.498 |
LIG_UBA3_1 | 68 | 77 | PF00899 | 0.516 |
MOD_CDK_SPK_2 | 331 | 336 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 513 | 520 | PF00069 | 0.465 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.705 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.371 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.521 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.336 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.515 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.357 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.468 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.658 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.682 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.473 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.484 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.467 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.320 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.308 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.608 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.443 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.777 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.759 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.651 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.681 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.753 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.458 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.633 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.555 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.381 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.459 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.387 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.455 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.589 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.461 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.446 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.525 |
MOD_N-GLC_1 | 233 | 238 | PF02516 | 0.771 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.491 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.517 |
MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.392 |
MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.366 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.467 |
MOD_N-GLC_2 | 149 | 151 | PF02516 | 0.185 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.528 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.636 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.408 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.377 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.373 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.496 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.452 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.385 |
MOD_NEK2_2 | 499 | 504 | PF00069 | 0.294 |
MOD_NEK2_2 | 509 | 514 | PF00069 | 0.445 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.385 |
MOD_PKA_1 | 156 | 162 | PF00069 | 0.547 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.531 |
MOD_PKA_2 | 493 | 499 | PF00069 | 0.502 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.554 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.568 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.476 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.439 |
MOD_Plk_1 | 463 | 469 | PF00069 | 0.502 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.516 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.501 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.513 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.377 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.493 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.336 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.297 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.502 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.447 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.442 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.468 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.447 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.446 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.461 |
MOD_SUMO_rev_2 | 201 | 209 | PF00179 | 0.711 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.621 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 553 | 556 | PF00400 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUB1 | Leptomonas seymouri | 60% | 100% |
A0A0S4KLR3 | Bodo saltans | 28% | 100% |
A0A1X0NS60 | Trypanosomatidae | 34% | 100% |
A0A3S7WZV3 | Leishmania donovani | 73% | 100% |
A0A422NIT0 | Trypanosoma rangeli | 34% | 100% |
A4I269 | Leishmania infantum | 73% | 100% |
C9ZRS8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AYB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4Q954 | Leishmania major | 74% | 99% |
V5BEB9 | Trypanosoma cruzi | 33% | 100% |