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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HMM6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.715 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.644 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.756 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.686 |
CLV_PCSK_FUR_1 | 6 | 10 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.685 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.818 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.632 |
DOC_ANK_TNKS_1 | 15 | 22 | PF00023 | 0.510 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.749 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.779 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 136 | 143 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 192 | 197 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 434 | 441 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 447 | 452 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 462 | 471 | PF00244 | 0.728 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.718 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.581 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.738 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.672 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.577 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.545 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.621 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.522 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.638 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.614 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.589 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.795 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.752 |
LIG_Integrin_RGD_1 | 426 | 428 | PF01839 | 0.563 |
LIG_LIR_Apic_2 | 209 | 213 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 226 | 232 | PF02991 | 0.704 |
LIG_LIR_Apic_2 | 329 | 334 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 65 | 74 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.501 |
LIG_Pex14_2 | 273 | 277 | PF04695 | 0.605 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.554 |
LIG_SH2_NCK_1 | 331 | 335 | PF00017 | 0.554 |
LIG_SH2_PTP2 | 97 | 100 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 358 | 362 | PF00017 | 0.515 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.643 |
LIG_SH2_STAT3 | 170 | 173 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.563 |
LIG_SUMO_SIM_anti_2 | 467 | 474 | PF11976 | 0.525 |
LIG_TYR_ITIM | 64 | 69 | PF00017 | 0.438 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.779 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.703 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.744 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.559 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.781 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.649 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.775 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.636 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.541 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.772 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.537 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.704 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.584 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.676 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.710 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.788 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.705 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.361 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.665 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.664 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.336 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.553 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.588 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.756 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.731 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.758 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.730 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.689 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.379 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.529 |
MOD_N-GLC_1 | 287 | 292 | PF02516 | 0.447 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.534 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.779 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.438 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.518 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.539 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.579 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.454 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.577 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.666 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.778 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.577 |
MOD_NEK2_2 | 316 | 321 | PF00069 | 0.391 |
MOD_OFUCOSY | 444 | 451 | PF10250 | 0.549 |
MOD_PIKK_1 | 462 | 468 | PF00454 | 0.555 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.701 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.419 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.357 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.654 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.817 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.664 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.543 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.712 |
MOD_PKA_2 | 461 | 467 | PF00069 | 0.779 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.438 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.532 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.666 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.389 |
MOD_Plk_2-3 | 404 | 410 | PF00069 | 0.744 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.640 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.427 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.240 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.725 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.391 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.574 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 238 | 247 | PF00179 | 0.545 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.451 |
TRG_ER_diArg_1 | 309 | 311 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 4 | 6 | PF00400 | 0.765 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.786 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZT1 | Leptomonas seymouri | 54% | 100% |
A0A0S4JH24 | Bodo saltans | 38% | 100% |
A0A3Q8IJ10 | Leishmania donovani | 73% | 100% |
A0A422NNS8 | Trypanosoma rangeli | 41% | 100% |
A4IBA4 | Leishmania infantum | 73% | 100% |
E9AF28 | Leishmania major | 73% | 98% |
E9B684 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |