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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3Q8IL99
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 94 | 98 | PF00656 | 0.773 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 139 | 143 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 464 | 466 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.535 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 464 | 466 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 141 | 147 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.713 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.585 |
CLV_Separin_Metazoa | 148 | 152 | PF03568 | 0.594 |
DEG_Kelch_Keap1_1 | 104 | 109 | PF01344 | 0.626 |
DEG_SCF_FBW7_1 | 158 | 163 | PF00400 | 0.448 |
DEG_SCF_FBW7_2 | 171 | 178 | PF00400 | 0.554 |
DEG_SPOP_SBC_1 | 28 | 32 | PF00917 | 0.650 |
DOC_CKS1_1 | 157 | 162 | PF01111 | 0.463 |
DOC_CKS1_1 | 172 | 177 | PF01111 | 0.551 |
DOC_CKS1_1 | 404 | 409 | PF01111 | 0.654 |
DOC_MAPK_gen_1 | 140 | 152 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 225 | 231 | PF00069 | 0.607 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.609 |
DOC_MAPK_gen_1 | 454 | 462 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 383 | 391 | PF00069 | 0.631 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.664 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.489 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 379 | 383 | PF12436 | 0.645 |
DOC_USP7_UBL2_3 | 464 | 468 | PF12436 | 0.399 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 13 | 19 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 170 | 175 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 384 | 390 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 413 | 422 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 454 | 460 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.541 |
LIG_BRCT_BRCA1_1 | 88 | 92 | PF00533 | 0.564 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.596 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.469 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.756 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.649 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.623 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.523 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.490 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.481 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.451 |
LIG_FHA_2 | 516 | 522 | PF00498 | 0.456 |
LIG_LIR_Apic_2 | 155 | 160 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 351 | 356 | PF02991 | 0.672 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 472 | 480 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 153 | 157 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 516 | 522 | PF02991 | 0.445 |
LIG_MLH1_MIPbox_1 | 88 | 92 | PF16413 | 0.564 |
LIG_PCNA_yPIPBox_3 | 320 | 334 | PF02747 | 0.467 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.677 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.584 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.641 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.572 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.623 |
LIG_SxIP_EBH_1 | 215 | 226 | PF03271 | 0.503 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.510 |
LIG_UBA3_1 | 459 | 464 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 330 | 335 | PF05994 | 0.524 |
LIG_WW_3 | 80 | 84 | PF00397 | 0.538 |
MOD_CDK_SPxK_1 | 261 | 267 | PF00069 | 0.537 |
MOD_CDK_SPxK_1 | 77 | 83 | PF00069 | 0.472 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.682 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.586 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.657 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.691 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.622 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.795 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.609 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.574 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.483 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.478 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.731 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.515 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.612 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.496 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.457 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.626 |
MOD_GlcNHglycan | 128 | 132 | PF01048 | 0.639 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.700 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.705 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.662 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.688 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.635 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.661 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.669 |
MOD_GlcNHglycan | 373 | 377 | PF01048 | 0.777 |
MOD_GlcNHglycan | 394 | 398 | PF01048 | 0.669 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.625 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.623 |
MOD_GlcNHglycan | 432 | 436 | PF01048 | 0.431 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.599 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.594 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.506 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.638 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.650 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.769 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.639 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.662 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.686 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.585 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.465 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.556 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.600 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.665 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.667 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.573 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.587 |
MOD_NEK2_1 | 266 | 271 | PF00069 | 0.632 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.451 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.413 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.570 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.537 |
MOD_PIKK_1 | 474 | 480 | PF00454 | 0.639 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.310 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.713 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.529 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.556 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.525 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.592 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.576 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.566 |
MOD_Plk_2-3 | 272 | 278 | PF00069 | 0.616 |
MOD_Plk_2-3 | 433 | 439 | PF00069 | 0.389 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.616 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.460 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.490 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.499 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.543 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.600 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.537 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.654 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.593 |
MOD_SUMO_rev_2 | 269 | 276 | PF00179 | 0.580 |
TRG_DiLeu_BaEn_2 | 152 | 158 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.620 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.640 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 360 | 362 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.590 |
TRG_NLS_Bipartite_1 | 122 | 144 | PF00514 | 0.636 |
TRG_NLS_MonoCore_2 | 138 | 143 | PF00514 | 0.668 |
TRG_NLS_MonoExtC_3 | 138 | 143 | PF00514 | 0.668 |
TRG_NLS_MonoExtN_4 | 139 | 144 | PF00514 | 0.664 |
TRG_Pf-PMV_PEXEL_1 | 226 | 230 | PF00026 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P596 | Leptomonas seymouri | 42% | 96% |
A4HKN0 | Leishmania braziliensis | 73% | 100% |
A4I857 | Leishmania infantum | 99% | 100% |
D0AAC7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9B318 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q536 | Leishmania major | 89% | 100% |