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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AZF4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 194 | 198 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.585 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.591 |
CLV_PCSK_PC7_1 | 314 | 320 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 72 | 76 | PF00082 | 0.407 |
DEG_APCC_DBOX_1 | 343 | 351 | PF00400 | 0.500 |
DEG_COP1_1 | 387 | 397 | PF00400 | 0.462 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.646 |
DEG_SCF_FBW7_1 | 405 | 412 | PF00400 | 0.452 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.511 |
DOC_MAPK_gen_1 | 113 | 123 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.626 |
DOC_PP4_FxxP_1 | 228 | 231 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.765 |
DOC_USP7_UBL2_3 | 113 | 117 | PF12436 | 0.455 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 115 | 123 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 260 | 270 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 318 | 325 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 341 | 351 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.503 |
LIG_BIR_III_4 | 212 | 216 | PF00653 | 0.438 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.632 |
LIG_deltaCOP1_diTrp_1 | 439 | 443 | PF00928 | 0.633 |
LIG_EH_1 | 354 | 358 | PF12763 | 0.350 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.299 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.586 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.431 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.547 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.407 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.634 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.527 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.585 |
LIG_LIR_Apic_2 | 227 | 231 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 223 | 233 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 415 | 426 | PF02991 | 0.616 |
LIG_LIR_Gen_1 | 438 | 447 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 223 | 228 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.613 |
LIG_PCNA_PIPBox_1 | 340 | 349 | PF02747 | 0.442 |
LIG_PCNA_yPIPBox_3 | 28 | 38 | PF02747 | 0.496 |
LIG_SH2_PTP2 | 281 | 284 | PF00017 | 0.452 |
LIG_SH2_PTP2 | 418 | 421 | PF00017 | 0.614 |
LIG_SH2_SRC | 281 | 284 | PF00017 | 0.452 |
LIG_SH2_SRC | 91 | 94 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 225 | 229 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.678 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.471 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.527 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 172 | 179 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 362 | 370 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 54 | 59 | PF11976 | 0.564 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.634 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.476 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.547 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.568 |
LIG_UBA3_1 | 66 | 75 | PF00899 | 0.457 |
LIG_WRC_WIRS_1 | 225 | 230 | PF05994 | 0.495 |
LIG_WW_2 | 232 | 235 | PF00397 | 0.413 |
MOD_CDK_SPK_2 | 405 | 410 | PF00069 | 0.511 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.540 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.727 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.599 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.580 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.550 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.452 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.313 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.453 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.605 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.488 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.465 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.587 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.579 |
MOD_GlcNHglycan | 211 | 216 | PF01048 | 0.597 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.568 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.586 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.563 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.669 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.632 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.486 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.673 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.545 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.430 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.462 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.620 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.763 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.461 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.536 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.564 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.497 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.457 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.644 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.515 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.530 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.397 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.498 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.425 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.337 |
MOD_NEK2_2 | 329 | 334 | PF00069 | 0.351 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.487 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.489 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.574 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.449 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.456 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.597 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.530 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.506 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.438 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.528 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.727 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.592 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.508 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.463 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.526 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.605 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.525 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.511 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.525 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.690 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.560 |
MOD_Plk_4 | 363 | 369 | PF00069 | 0.400 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.677 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.482 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.342 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.682 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.645 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.734 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.705 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.539 |
TRG_DiLeu_BaEn_1 | 363 | 368 | PF01217 | 0.307 |
TRG_DiLeu_BaEn_1 | 52 | 57 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_3 | 203 | 209 | PF01217 | 0.455 |
TRG_DiLeu_BaEn_4 | 286 | 292 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.614 |
TRG_ER_diArg_1 | 192 | 195 | PF00400 | 0.728 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.527 |
TRG_NES_CRM1_1 | 362 | 375 | PF08389 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.540 |
TRG_Pf-PMV_PEXEL_1 | 146 | 150 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IB83 | Leptomonas seymouri | 48% | 100% |
A0A1X0NF90 | Trypanosomatidae | 27% | 100% |
A0A3R7KL96 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X122 | Leishmania donovani | 88% | 100% |
A4HG25 | Leishmania braziliensis | 72% | 99% |
A4I346 | Leishmania infantum | 88% | 100% |
C9ZJL9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9ACW5 | Leishmania major | 88% | 100% |
V5BB13 | Trypanosoma cruzi | 26% | 100% |